Clinical Research Coordinator I Job at Mount Sinai Health System (New York)

Clinical Research Coordinator I

Supports Frenova Renal Research by providing administrative and clinical support...

Location

United States of America , Mishawaka

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

High School Diploma required
Associate’s Degree or Certified Medical Assistant preferred
2-4 years of experience of related experience preferred
Minimum 18 months experience in a medical setting and/or clinical research setting required
Willingness to obtain research specific training as needed
Ability to meet deadlines for multiple concurrent projects
Ability to understand and follow study specific protocol and direction
Ability to understand a patient medical record
Attention to detail required
Good computer skills including MS Excel

Job Responsibility

Utilizes experience and knowledge to act as a resource and provide on-going leadership and support to Clinical Research Assistant I
Conducts on the job training for Clinical Research Assistant I as requested
Researches and identifies research related issues and discrepancies
Obtains and prepares regulatory/essential documents throughout the duration of a study
Ensures documents and forms are compiled and submitted in a timely manner
Assists with maintaining constant communication with Institutional Review Boards, study sponsors, dialysis facility, practice and field staff
Assists with the contracting process, document preparation and execution
Interfaces with potential study subjects for the purpose of promoting participation in research studies
Assists with screening subjects for participation eligibility
Assists with and documents the obtaining of informed consent according to GCP

What we offer

Healthcare
Continuing Education
Paid Time Off
Collaborative Environment
Additional Perks
401(k) Retirement Saving

Fulltime

Clinical Research Coordinator I

CRC I is an entry-level position responsible for serving as the primary coordina...

Location

United States , Tucson

Salary:

Not provided

Tucson Medical Center

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a relevant field or equivalent experience
Good Clinical Practice, Human Research Protection Training, and Basic Life Support certifications required within 30 days of start date
Ability to understand clinical research theory, practices, and tools utilized
Above-average skill in the use of all Microsoft Office applications
Proficient with technology and comfortable learning new protocols, electronic data capture (EDC) systems, and electronic medical records (EMRs)
Knowledge of clinical care and assessment best practices
Knowledge of regulations and policies as they relate to patient research, evaluation, care, and information
Ability to maintain investigational product accountability
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
Ability to read, analyze, and interpret professional journals, technical procedures, or governmental regulations

Job Responsibility

Oversees, coordinates, develops, and manages the day-to-day clinical activities for specified research trials
Facilitate and coordinate daily clinical activities
Act as liaison between PI’s, ancillary departments, research subjects, sponsoring organizations and regulating bodies, vendors, brokers, and suppliers
Maintain regulatory documentation, including the Investigator Site File (ISF)
Prepare, submit, and track Institutional Review Board (IRB) submissions, amendments, and reports
Ensure investigational product (IP) accountability throughout the study
Coordinate study and Research Staff compliance metrics
Coordinate participant recruitment and outreach programs
Coordinate department quality and data integrity programs
Support research billing compliance and invoicing/financial administration

Fulltime

Clinical Research Coordinator I

The Clinical Research Coordinator I assists principal investigators or other stu...

Location

United States , Los Angeles

Salary:

61152.00 - 100464.00 USD / Year

Children's Hospital Los Angeles

Expiration Date

Until further notice

Requirements

1+ year experience in clinical trial coordination or computerized databases
High School Diploma or GED required
Bachelor's degree or Associate degree in related scientific field preferred
Certified clinical research associate/coordinator preferred

Job Responsibility

Assists principal investigators or other study team members with research studies
Assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects

What we offer

Competitive compensation package
Robust benefits program

Fulltime

Clinical Research Coordinator I-Neurosurgery

The Clinical Research Coordinator assists in the daily activities of clinical re...

Location

United States , New York

Salary:

58661.00 - 73530.00 USD / Year

Mount Sinai Health System

Expiration Date

Until further notice

Requirements

Bachelors or Masters degree in Science or closely related field
No experience required
One year of research experience preferred

Job Responsibility

Collects and records study data. Inputs all information into database
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements
Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires
Assists in preparing grant applications, IRB/GCO for submission and filings
Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews
Secures, delivers and ships clinical specimens as required by the protocol
Prepares for monitoring visits
Performs other related duties

Clinical Research Coordinator – Neurophysiology Research Core (CNRC)

The Clinical Research Coordinator will play a primary role in collecting data fo...

Location

United States , Brookline

Salary:

44657.60 - 69773.60 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

A Bachelor's degree is required
2 years of experience is required
Previous experience with children with autism or other neurodevelopmental conditions is ideal
Previous experience working in a research setting (preferably paid professional experience, but may include undergraduate research experiences) is also a plus.

Job Responsibility

Consents and recruits patients for research studies through personal interviews and written communications with patients/families
Provides detailed background information regarding studies to families, communicates all policies and procedures, and responds to all inquiries
Evaluates suitability of prospective study candidates and makes selections based upon clinical knowledge of each study
Performs EEG and other data collection methods (e.g., ERP, eye-tracking) on participants aged 0-65 years
Serves as liaison to the families/patients in the research studies, conducted at both on-site and off-site locations, guiding and advising them during data collection
Acts as a resource to study participants, addressing any concerns they may have
Troubleshoots resolution of any issues that may arise during data collection
Participates in the training of newly hired research study assistants, as required
Coordinates activities between the hospital and research laboratories to ensure correct testing/processing and send out instructions specific to the study
Communicates project policies and procedures to personnel

What we offer

flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

Clinical Research Coordinator

Investigators in the Division of Cancer Genetics and Prevention at the Dana-Farb...

Location

United States , Boston

Salary:

48100.00 - 54400.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Bachelor's degree required, with a focus in public health, social science, or natural science preferred
0-1 years of research experience required, with experience in a clinical or scientific setting strongly preferred
Effective in working independently and as part of a team
Comfortable with patient and clinical staff interaction and handling research specimens (e.g. saliva, blood, tissue, and/or urine)
Excellent interpersonal skills and the ability to communicate and relate effectively with diverse groups
Detail-oriented with excellent organizational, communication, problem-solving, and time management skills
Strong computer skills, including proficiency with Microsoft Office products, knowledge or ability to learn other systems such as Epic and REDCap
Competencies in study data entry and/or CRF completion, research study coordination, and regulatory requirements
Dependable, motivated, and willing to learn new processes and procedures as needed
Ability to approach projects in a responsible, thoughtful, and thorough manner

Job Responsibility

Responsible for participant recruitment, data reporting and management, collection of source documents, use and development of case report forms, adverse event reporting, filing and archiving of study records, and resolution of data queries
Interact with study participants as directed/required by the protocol and/or study team
Ensure all study related samples are collected, properly prepared and shipped according to the protocol requirements and IATA/DOT regulations
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits
Coordination and management of studies, including communication with regulatory authorities
Close-out of studies, including contributing to research articles, audit preparation, and communication with regulatory agencies
Facilitation of blood and tissue specimen collection processes, with potential travel needed to other local institutions via shuttle network

Fulltime

Clinical Research Coordinator II

Must be comfortable with 50% travel. Highly prefer someone who lives in the Nort...

Location

United States

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

2 to 4 years of clinical research experience, or has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures
Critical care, nephrology and/ or cardiac experience desirable
Willing to pursue CCRC or CCRP certification when eligible
Current state licensure, if applicable
Good computer skills: Microsoft Office minimally
Excellent communication and organizational skills
Ability to work independently, and exhibit diplomacy and problem solving skills in the performance of this role

Job Responsibility

Assists with the determination of the guidelines for the collection of clinical data and coordinates and implements procedures and processes for data collection
Coordinates all aspects of study subject care from pre-screening through study completion as defined by the protocol and Principal Investigator (PI) delegation
Protect the rights and the well-being of subjects enrolled in studies
Ensures thorough, individualized, protocol-based study subject education on all study process requirements including but not limited to: informed consent, study participation obligations, appropriate use of investigational product, safety, privacy, rights and responsibilities
Develops processes for methodically monitoring the status of study subjects as they progress through the study’s timeline of activities
Regularly evaluates the study subjects’ condition and communicates/documents concerns to PI to ensure subject safety
Accurately documents study subject activities as outlined by the protocol
Maintains documents according to applicable HIPAA and regulatory requirements
Implements study-specific quality goals and practices
Acts as the point of contact or lead person in a facility/practice to oversee protocol compliance

Clinical Research Coordinator

Responsible for supporting the Research leadership and Principal Investigator of...

Location

United States , Boca Raton

Salary:

Not provided

Baptist Health

Expiration Date

Until further notice

Requirements

Associate's of arts degree is required
In lieu of Associates degree, 3 years of research experience is required OR, a Foreign Medical Degree with 1 year of experience required
Advanced computer literacy in Microsoft Office
Proven ability to manage multiple assignments systematically
Excellent interpersonal, collaborative, and team-building skills are required
Must be able to work in a high-demand environment with the ability to take responsibility in meeting deadlines
Strong verbal and written communication skills
Minimum Required Experience: 2 Years

Job Responsibility

Supporting the Research leadership and Principal Investigator of a designated research project
Performing functions required by the research protocols with attention to participant safety
Ensuring that all requirements of the protocol are met, while meeting compliance with regulatory standards and FDA requirements for each protocol
Completing detailed paperwork in strict accordance with regulatory requirements
Collaborating with physicians, patients, sponsors, and other departments in a service excellence manner

What we offer

Career growth and development opportunities, with clear pathways and ongoing support
Comprehensive health and wellness resources that go beyond traditional benefits
A wellness program that can help employees eliminate their medical plan deductible, reducing out-of-pocket healthcare costs
Tuition reimbursement to support continued learning and advancement

Fulltime

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Clinical Research Coordinator I

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